2,048 recalls tagged with “cpsc regulated”.
NOW Foods recalled 1,689 10 oz pouches of NOW Real Food Organic Unsalted Whole Raw Cashews nationwide after undeclared pine nuts were detected. The hazard poses an allergen risk. Consumers who bought this product should stop using it and contact NOW Foods for a refund or replacement.
Orwashers brand Soho Sourdough XL Batard is being recalled after labeling errors could hide sesame seeds. The recall covers 4 pallets of 6 pieces per case in Massachusetts. Consumers should avoid consumption and contact Oven Artisans LLC for refunds or replacements.
Biomet recalled 98 ZipTight Acute AC Joint Implant Single Ziploop devices on Sept. 23, 2025. A missing slotted button assembly was identified in one lot. Healthcare providers and patients should stop using the device immediately and follow Biomet’s recall instructions.
BD MAX System recall affects 62 units distributed worldwide in 2025 after unauthorized access to service credentials. An unauthorized actor accessed credentials used by BD technical support teams. Healthcare providers should stop using the devices and follow the manufacturer’s recall instructions.
BD recalled 2,050 units of the EpiCenter Microbiology Data Management System due to unauthorized access to product service credentials. The defect could allow access to confidential data. Stop using affected devices and follow manufacturer guidance for updates or replacement.
Southwind Foods LLC dba Great American Seafood Imports Co. expanded recall covers Arctic Shores, Best Yet, Great American and Master Catch frozen shrimp sold nationwide by multiple retailers after Cesium-137 contamination was detected. The contaminated product was manufactured under insanitary conditions. Consumers should not eat the product and should contact the company for refunds or replaced.
Tengen USA Trading Corp recalled 26 cases of YO!MAN Cucumber (Fresh Hunan Flavor) on September 23, 2025, due to undeclared cyclamates. The product poses a high risk of poisoning for consumers allergic to this chemical. Consumers should not consume the product and seek refunds.
BD recalled 1,086 BD BACTEC Blood Culture System units worldwide after unauthorized access to product service credentials. The breach could compromise confidentiality, integrity and availability of affected devices and data. Hospitals and healthcare providers should stop using the device immediately and follow BD’s recall instructions.
BD recalled 4,283 Phoenix M50 Automated Microbiology Systems worldwide after unauthorized access to product service credentials. The unauthorized actor could access affected products and data. Labs should stop using these devices and follow the recall instructions from BD; contact BD for remediation guidance.
Great American Seafood Imports recalled 93,122 cases of its frozen raw shrimp skewers after potential Cs-137 contamination. The recall expansion cites insanitary manufacturing conditions. Consumers should not consume the product and should contact the company for refund or replacement.
Arctic Shores recalled 93,122 cases of Frozen cooked salad shrimp in 6 oz bags. The recall affects products distributed to 26 states. The product may be contaminated with Cesium-137 due to insanitary manufacturing conditions. Consumers should not eat this product and should contact Southwind Foods LLC dba Great American Seafood Imports for refund or replacement information.
Sea Port brand Raw Frozen Easy Peel Headless Shell-On White Shrimp, Jumbo 16-20, distributed by Sea Port Products Corp in Kirkland, WA, is recalled. A Cs-137 contamination risk is identified. About 1,800 cases are affected across two master-case configurations. Consumers should not consume the product and should contact Sea Port for refunds or replacements.
Ascend Laboratories recalled Atorvastatin Calcium Tablets USP 40 mg, 90-count (NDC 67877-513-90), 500-count (NDC 67877-513-05), and 1,000-count (NDC 67877-513-10) nationwide in the United States. The batches failed dissolution specifications. Patients should stop using the medication and contact Ascend Laboratories, LLC or their healthcare provider for guidance.
Kico Knee Innovation recalls 21 ARVIS Shoulder systems nationwide after reports that AI planning software may cause implant malalignment or reduced range of motion. The recall covers software version V2025.1.2 used with IN-27300 hardware. Healthcare providers and patients should stop using the device and follow manufacturer instructions.
Beckman Coulter recalls 160 DxC 500i Clinical Analyzer Modules and the DxI 9000 Access Immunoassay Analyzer worldwide after a software anomaly could misapply manual dilution factors. The defect affects samples already in progress using the same Sample ID. Stop using the devices immediately and follow the recall instructions. Beckman Coulter will provide instructions via the recall process.
Black Sheep Egg Company recalled 20,625 dozen eggs sold at retail and wholesale locations in Arkansas and Missouri after a potential Salmonella contamination. The eggs are Free Range Grade AA Large Brown, loose-packed in boxes. Consumers should not consume these eggs and should contact Black Sheep Egg Company for refunds or replacements.
Black Sheep Egg Company recalled 46,800 dozen Free Range Grade AA Medium White Eggs sold at retail and wholesale outlets in Arkansas and Missouri. The FDA recall cites potential Salmonella contamination. Consumers should not consume the eggs and should contact Black Sheep Egg Company for refund or replacement.
Beckman Coulter recalled 571 DxI 9000 Access Immunoassay Analyzers and DxC 500i Clinical Analyzers distributed worldwide. A software anomaly may prevent correct application of manual dilution factors for tests already in progress on the same Sample ID. Labs should stop using the devices immediately and follow recall instructions.
Black Sheep Egg Company recalled 23,400 dozen Free Range Grade AA Large White Eggs sold at retail and wholesale locations in Arkansas and Missouri due to potential Salmonella contamination. Consumers should not eat these eggs. Contact Black Sheep Egg Company, LLC for refund or replacement information.
Ascend Laboratories recalls Atorvastatin Calcium Tablets USP, 80 mg, in 90-count and 500-count packages nationwide. The recall cites failed dissolution specifications. Health care providers and patients should stop using the recalled tablets and seek guidance from Ascend or their prescribers.